Identity
- Trade Name
- MeDiCa FDA UDI
- Generic Name
- Native DNA antibody (anti-nDNA) IVD, kit, fluorescent immunoassay FDA UDI
- Device Name
- A-nDNA-A Crithidia luciliae 48 Test Kit FDA UDI
- Model / Reference
- 2001-48 FDA UDI
- Description
- A-nDNA-A Crithidia luciliae 48 Test Kit FDA UDI
Identifiers
- Catalog Number
- 2001-48 FDA UDI
- Primary DI / UDI-DI
- 00813545026929 FDA UDI
- 510(k) Number
- K790106 FDA UDI
- FDA Product Code
- DHC FDA UDI
- GMDN Term
- Native DNA antibody (anti-nDNA) IVD, kit, fluorescent immunoassay FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.5820 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Native DNA antibody (anti-nDNA) IVD, kit, fluorescent immunoassay
MeDiCa by Scimedx Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Native DNA antibody (anti-nDNA) IVD, kit, fluorescent immunoassay.
- IgG Anti-nDNA Fluorescent Test System — IMMUNO CONCEPTS INC
- IFA nDNA Test System — ZEUS SCIENTIFIC, INC.
- Anti-nDNA IgG IFA 96 Test — HEMAGEN DIAGNOSTICS, INC. · Class II
- IgG Anti-nDNA Fluorescent Test System — IMMUNO CONCEPTS INC
- IMMCO DIAGNOSTICS — Immco Diagnostics, Inc. · Class II
- Fluorescent nDNA Test System — IMMUNO CONCEPTS INC
- IgG Anti-nDNA Fluorescent Test System — IMMUNO CONCEPTS INC
- IgG Anti-nDNA Fluorescent Test System — IMMUNO CONCEPTS INC
Cleared under the same submission
K790106 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Scimedx Corp.
Sources (1)
- FDA UDI 2bbe65f1-72ee-4800-b2b7-173db267b085 36 fields · synced May 30, 2026